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Items: 45


Detection of 6 TFEB-amplified renal cell carcinomas and 25 renal cell carcinomas with MITF translocations: systematic morphologic analysis of 85 cases evaluated by clinical TFE3 and TFEB FISH assays.

Skala SL, Xiao H, Udager AM, Dhanasekaran SM, Shukla S, Zhang Y, Landau C, Shao L, Roulston D, Wang L, Siddiqui J, Cao X, Magi-Galluzzi C, Zhang M, Osunkoya AO, Smith SC, McKenney JK, Betz BL, Myers JL, Chinnaiyan AM, Tomlins SA, Mehra R.

Mod Pathol. 2018 Jan;31(1):179-197. doi: 10.1038/modpathol.2017.99. Epub 2017 Aug 25.


Randomized Phase II Study of Azacitidine Alone or in Combination With Lenalidomide or With Vorinostat in Higher-Risk Myelodysplastic Syndromes and Chronic Myelomonocytic Leukemia: North American Intergroup Study SWOG S1117.

Sekeres MA, Othus M, List AF, Odenike O, Stone RM, Gore SD, Litzow MR, Buckstein R, Fang M, Roulston D, Bloomfield CD, Moseley A, Nazha A, Zhang Y, Velasco MR, Gaur R, Atallah E, Attar EC, Cook EK, Cull AH, Rauh MJ, Appelbaum FR, Erba HP.

J Clin Oncol. 2017 Aug 20;35(24):2745-2753. doi: 10.1200/JCO.2015.66.2510. Epub 2017 May 9.


Genome-Wide Single-Nucleotide Polymorphism Array Analysis Improves Prognostication of Acute Lymphoblastic Leukemia/Lymphoma.

Wang Y, Miller S, Roulston D, Bixby D, Shao L.

J Mol Diagn. 2016 Jul;18(4):595-603. doi: 10.1016/j.jmoldx.2016.03.004. Epub 2016 May 6.


Cytogenetic, fluorescence in situ hybridization, and genomic array characterization of chronic myeloid leukemia with cryptic BCR-ABL1 fusions.

Shao L, Miller S, Keller-Ramey J, Zhang Y, Roulston D.

Cancer Genet. 2015 Jul-Aug;208(7-8):396-403. doi: 10.1016/j.cancergen.2015.04.006. Epub 2015 Apr 25.


Mutations in linker histone genes HIST1H1 B, C, D, and E; OCT2 (POU2F2); IRF8; and ARID1A underlying the pathogenesis of follicular lymphoma.

Li H, Kaminski MS, Li Y, Yildiz M, Ouillette P, Jones S, Fox H, Jacobi K, Saiya-Cork K, Bixby D, Lebovic D, Roulston D, Shedden K, Sabel M, Marentette L, Cimmino V, Chang AE, Malek SN.

Blood. 2014 Mar 6;123(10):1487-98. doi: 10.1182/blood-2013-05-500264. Epub 2014 Jan 16.


The Challenge of t (6;9) and FLT3-Positive Acute Myelogenous Leukemia in a Young Adult.

Song Y, Bixby D, Roulston D, Magenau J, Choi SW.

J Leuk (Los Angel). 2014;2. pii: 1000167.


Undifferentiated small round cell sarcoma with t(4;19)(q35;q13.1) CIC-DUX4 fusion: a novel highly aggressive soft tissue tumor with distinctive histopathology.

Choi EY, Thomas DG, McHugh JB, Patel RM, Roulston D, Schuetze SM, Chugh R, Biermann JS, Lucas DR.

Am J Surg Pathol. 2013 Sep;37(9):1379-86. doi: 10.1097/PAS.0b013e318297a57d.


Analysis of de novo HOXA13 polyalanine expansions supports replication slippage without repair in their generation.

Owens KM, Quinonez SC, Thomas PE, Keegan CE, Lefebvre N, Roulston D, Larsen CA, Stadler HS, Innis JW.

Am J Med Genet A. 2013 May;161A(5):1019-27. doi: 10.1002/ajmg.a.35843. Epub 2013 Mar 26.


Clonal evolution and devolution after chemotherapy in adult acute myelogenous leukemia.

Parkin B, Ouillette P, Li Y, Keller J, Lam C, Roulston D, Li C, Shedden K, Malek SN.

Blood. 2013 Jan 10;121(2):369-77. doi: 10.1182/blood-2012-04-427039. Epub 2012 Nov 21.


Concomitant BCR-ABL1 translocation and JAK2(V617F) mutation in three patients with myeloproliferative neoplasms.

Hummel JM, Kletecka MC, Sanks JK, Chiselite MD, Roulston D, Smith LB, Czuchlewski DR, Elenitoba-Johnson KS, Lim MS.

Diagn Mol Pathol. 2012 Sep;21(3):176-83. doi: 10.1097/PDM.0b013e318246975e.


Treatment-influenced associations of PML-RARα mutations, FLT3 mutations, and additional chromosome abnormalities in relapsed acute promyelocytic leukemia.

Gallagher RE, Moser BK, Racevskis J, Poiré X, Bloomfield CD, Carroll AJ, Ketterling RP, Roulston D, Schachter-Tokarz E, Zhou DC, Chen IM, Harvey R, Koval G, Sher DA, Feusner JH, Tallman MS, Larson RA, Powell BL, Appelbaum FR, Paietta E, Willman CL, Stock W.

Blood. 2012 Sep 6;120(10):2098-108. doi: 10.1182/blood-2012-01-407601. Epub 2012 Jun 25.


Spontaneous remission of congenital acute myeloid leukemia with t(8;16)(p11;13).

Wu X, Sulavik D, Roulston D, Lim MS.

Pediatr Blood Cancer. 2011 Feb;56(2):331-2. doi: 10.1002/pbc.22859. Epub 2010 Nov 28. No abstract available.


Acquired genomic copy number aberrations and survival in adult acute myelogenous leukemia.

Parkin B, Erba H, Ouillette P, Roulston D, Purkayastha A, Karp J, Talpaz M, Kujawski L, Shakhan S, Li C, Shedden K, Malek SN.

Blood. 2010 Dec 2;116(23):4958-67. doi: 10.1182/blood-2010-01-266999. Epub 2010 Aug 20.


Prognostic impact of monosomal karyotype in young adult and elderly acute myeloid leukemia: the Southwest Oncology Group (SWOG) experience.

Medeiros BC, Othus M, Fang M, Roulston D, Appelbaum FR.

Blood. 2010 Sep 30;116(13):2224-8. doi: 10.1182/blood-2010-02-270330. Epub 2010 Jun 18.


NF1 inactivation in adult acute myelogenous leukemia.

Parkin B, Ouillette P, Wang Y, Liu Y, Wright W, Roulston D, Purkayastha A, Dressel A, Karp J, Bockenstedt P, Al-Zoubi A, Talpaz M, Kujawski L, Liu Y, Shedden K, Shakhan S, Li C, Erba H, Malek SN.

Clin Cancer Res. 2010 Aug 15;16(16):4135-47. doi: 10.1158/1078-0432.CCR-09-2639. Epub 2010 May 26.


ON012380, a putative BCR-ABL kinase inhibitor with a unique mechanism of action in imatinib-resistant cells.

Wu J, Meng F, Ying Y, Peng Z, Daniels L, Bornmann WG, Quintás-Cardama A, Roulston D, Talpaz M, Peterson LF, Donato NJ.

Leukemia. 2010 Apr;24(4):869-72. doi: 10.1038/leu.2009.300. Epub 2010 Jan 28. No abstract available.


Myxoid malignant fibrous histiocytoma with multiple primary sites.

Muler JH, Paulino AF, Roulston D, Baker LH.

Sarcoma. 2002;6(1):51-5. doi: 10.1080/13577140220127567.


Undifferentiated small round cell sarcomas with rare EWS gene fusions: identification of a novel EWS-SP3 fusion and of additional cases with the EWS-ETV1 and EWS-FEV fusions.

Wang L, Bhargava R, Zheng T, Wexler L, Collins MH, Roulston D, Ladanyi M.

J Mol Diagn. 2007 Sep;9(4):498-509. Epub 2007 Aug 9.


Distinct classes of chromosomal rearrangements create oncogenic ETS gene fusions in prostate cancer.

Tomlins SA, Laxman B, Dhanasekaran SM, Helgeson BE, Cao X, Morris DS, Menon A, Jing X, Cao Q, Han B, Yu J, Wang L, Montie JE, Rubin MA, Pienta KJ, Roulston D, Shah RB, Varambally S, Mehra R, Chinnaiyan AM.

Nature. 2007 Aug 2;448(7153):595-9.


Specific extra chromosomes occur in a modal number dependent pattern in pediatric acute lymphoblastic leukemia.

Heerema NA, Raimondi SC, Anderson JR, Biegel J, Camitta BM, Cooley LD, Gaynon PS, Hirsch B, Magenis RE, McGavran L, Patil S, Pettenati MJ, Pullen J, Rao K, Roulston D, Schneider NR, Shuster JJ, Sanger W, Sutcliffe MJ, van Tuinen P, Watson MS, Carroll AJ.

Genes Chromosomes Cancer. 2007 Jul;46(7):684-93.


Human papillomavirus in amniotic fluid.

Ruffin MT 4th, Bailey JM, Roulston D, Lee DR, Tucker RA, Swan DC, Unger ER.

BMC Pregnancy Childbirth. 2006 Sep 4;6:28.


Peripheral primitive neuroectodermal tumor/Ewing's sarcoma of the craniospinal vault: case reports and review.

Mobley BC, Roulston D, Shah GV, Bijwaard KE, McKeever PE.

Hum Pathol. 2006 Jul;37(7):845-53. Epub 2006 May 19. Review.


TMPRSS2:ETV4 gene fusions define a third molecular subtype of prostate cancer.

Tomlins SA, Mehra R, Rhodes DR, Smith LR, Roulston D, Helgeson BE, Cao X, Wei JT, Rubin MA, Shah RB, Chinnaiyan AM.

Cancer Res. 2006 Apr 1;66(7):3396-400.


Burkitt lymphoma and Williams syndrome: a model for children with a multisystem disorder and malignancy.

Thornburg CD, Roulston D, Castle VP.

J Pediatr Hematol Oncol. 2005 Feb;27(2):109-11.


Stem cell transplantation in patients with severe congenital neutropenia with evidence of leukemic transformation.

Choi SW, Boxer LA, Pulsipher MA, Roulston D, Hutchinson RJ, Yanik GA, Cooke KR, Ferrara JL, Levine JE.

Bone Marrow Transplant. 2005 Mar;35(5):473-7.


A novel chromosomal inversion at 11q23 in infant acute myeloid leukemia fuses MLL to CALM, a gene that encodes a clathrin assembly protein.

Wechsler DS, Engstrom LD, Alexander BM, Motto DG, Roulston D.

Genes Chromosomes Cancer. 2003 Jan;36(1):26-36.


Localization of the chromosome 22 breakpoints in two cases of acute megakaryoblastic leukemia with t(1;22)(p13;q13).

Dickstein JI, Davis EM, Roulston D.

Cancer Genet Cytogenet. 2001 Sep;129(2):150-4.


Susceptibility gene for familial acute myeloid leukemia associated with loss of 5q and/or 7q is not localized on the commonly deleted portion of 5q.

Gao Q, Horwitz M, Roulston D, Hagos F, Zhao N, Freireich EJ, Golomb HM, Olopade OI.

Genes Chromosomes Cancer. 2000 Jun;28(2):164-72.


Spectral karyotype analysis of T-cell acute leukemia.

Rowley JD, Reshmi S, Carlson K, Roulston D.

Blood. 1999 Mar 15;93(6):2038-42.


CBFA2(AML1) translocations with novel partner chromosomes in myeloid leukemias: association with prior therapy.

Roulston D, Espinosa R 3rd, Nucifora G, Larson RA, Le Beau MM, Rowley JD.

Blood. 1998 Oct 15;92(8):2879-85.


Codeletion of CDKN2 and MTAP genes in a subset of non-Hodgkin's lymphoma may be associated with histologic transformation from low-grade to diffuse large-cell lymphoma.

Dreyling MH, Roulston D, Bohlander SK, Vardiman J, Olopade OI.

Genes Chromosomes Cancer. 1998 May;22(1):72-8. Review.


Pseudo-Gaucher histiocytes identified up to 1 year after transplantation for CML are BCR/ABL-positive.

Anastasi J, Musvee T, Roulston D, Domer PH, Larson RA, Vardiman JW.

Leukemia. 1998 Feb;12(2):233-7.


Familial myeloid leukemia associated with loss of the long arm of chromosome 5.

Olopade OI, Roulston D, Baker T, Narvid S, Le Beau MM, Freireich EJ, Larson RA, Golomb HM.

Leukemia. 1996 Apr;10(4):669-74.


Therapy-related acute leukemia associated with t(11q23) after primary acute myeloid leukemia with t(8;21): a report of two cases.

Roulston D, Anastasi J, Rudinsky R, Nucifora G, Zeleznik-Le N, Rowley JD, McGavran L, Tsuchida M, Hayashi Y.

Blood. 1995 Nov 1;86(9):3613-4. Review. No abstract available.


Correlation between cell morphology and expression of the AML1/ETO chimeric transcript in patients with acute myeloid leukemia without the t(8;21).

Nucifora G, Dickstein JI, Torbenson V, Roulston D, Rowley JD, Vardiman JW.

Leukemia. 1994 Sep;8(9):1533-8.


Consistent intergenic splicing and production of multiple transcripts between AML1 at 21q22 and unrelated genes at 3q26 in (3;21)(q26;q22) translocations.

Nucifora G, Begy CR, Kobayashi H, Roulston D, Claxton D, Pedersen-Bjergaard J, Parganas E, Ihle JN, Rowley JD.

Proc Natl Acad Sci U S A. 1994 Apr 26;91(9):4004-8.


Homozygous deletions within chromosomal bands 9p21-22 in bladder cancer.

Stadler WM, Sherman J, Bohlander SK, Roulston D, Dreyling M, Rukstalis D, Olopade OI.

Cancer Res. 1994 Apr 15;54(8):2060-3.


Molecular genetics of myeloid leukemia: identification of the commonly deleted segment of chromosome 20.

Roulston D, Espinosa R 3rd, Stoffel M, Bell GI, Le Beau MM.

Blood. 1993 Dec 1;82(11):3424-9.


Cytogenetic and molecular delineation of the smallest commonly deleted region of chromosome 5 in malignant myeloid diseases.

Le Beau MM, Espinosa R 3rd, Neuman WL, Stock W, Roulston D, Larson RA, Keinanen M, Westbrook CA.

Proc Natl Acad Sci U S A. 1993 Jun 15;90(12):5484-8.


Involvement of the AML1 gene in the t(3;21) in therapy-related leukemia and in chronic myeloid leukemia in blast crisis.

Nucifora G, Birn DJ, Espinosa R 3rd, Erickson P, LeBeau MM, Roulston D, McKeithan TW, Drabkin H, Rowley JD.

Blood. 1993 May 15;81(10):2728-34.


dNORs and meiotic nondisjunction.

Schwartz S, Roulston D, Cohen MM.

Am J Hum Genet. 1989 May;44(5):627-30. No abstract available.


Cytological and molecular studies of nucleolar organizing region variants and recombination in trisomy 21.

Roulston D, Antonarakis SE, Lewis JG, Cohen MM, Schwartz S.

Prog Clin Biol Res. 1989;311:81-100. No abstract available.


An autosomal-dominant form of juvenile periodontitis: its localization to chromosome 4 and linkage to dentinogenesis imperfecta and Gc.

Boughman JA, Halloran SL, Roulston D, Schwartz S, Suzuki JB, Weitkamp LR, Wenk RE, Wooten R, Cohen MM.

J Craniofac Genet Dev Biol. 1986;6(4):341-50.


Effect of carbamazepine on psychomotor performance in näive subjects.

MacPhee GJ, Goldie C, Roulston D, Potter L, Agnew E, Laidlaw J, Brodie MJ.

Eur J Clin Pharmacol. 1986;30(1):37-42.


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